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Interleukin 1 (IL-1) type I receptors mediate activation of rat hypothalamus-pituitary-adrenal axis and interleukin 6 production as shown by receptor type selective deletion mutants of IL-1β
被引:11
|作者:
Van Dam, AM
Malinowsky, D
Lenczowski, MJP
Bartfai, T
Tilders, FJH
机构:
[1] Free Univ Amsterdam, Fac Med, Dept Pharmacol, Res Inst Neurosci, NL-1081 BT Amsterdam, Netherlands
[2] Univ Stockholm, Dept Neurochem & Neurotoxicol, Stockholm, Sweden
来源:
关键词:
ACTH;
corticosterone;
deletion mutants;
interleukin;
1;
receptor;
D O I:
10.1006/cyto.1997.0315
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The cytokine interleukin 1 (IL-1) plays an important role in the activation of the hypothalamus-pituitary-adrenal (HPA)-axis and interleukin 6 (IL-6) production during infection or inflammation. Which of the interleukin 1 receptor types mediates these effects is not known. To investigate this issue a pharmacological approach chosen by using recently developed IL-1 receptor type selective ligands, Rats were given one of various doses of recombinant human IL-1 beta (rhIL-1 beta; 1 and 10 mu g/kg) and of several IL-1 beta mutants (Delta SND, Delta QGE and Delta I; 1, 10 and 100 mu g/kg), that differ in their affinities for the IL-1 type I receptor but have similar affinities for the IL-1 type II receptor. One hour after intravenous administration of rhIL-1 beta or IL-1 beta mutants, plasma levels of ACTH, corticosterone (cort) and IL-6 were measured. Doses of 1 and 10 mu g/kg rhIL-1 beta markedly elevated plasma levels of ACTH, cort and IL-6, However, 10-100-fold higher doses of IL-1 beta mutants Delta SND and Delta QGE and at least 100-fold higher doses of Delta I have to be administered to increase plasma levels of ACTH, cort and IL-6, The potency differences correlate with their respective affinity for the type I receptor but not with that of the IL-1 type II receptor. It is concluded that IL-1 beta induced ACTH, cort and IL-6 production is mediated by interleukin 1 type I receptors, (C) 1998 Academic Press Limited.
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页码:413 / 417
页数:5
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